Annals ofBioethics

Volume: 9 - Number: 96 - November 15, 2010

Outstanding

Reporting of euthanasia and physician-assisted suicide in the Netherlands: descriptive study

Survey of doctors\' opinions of the legalisation of physician assisted suicide

Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?

Assessment of the capacity to consent to treatment in patients admitted to acute medical wards

Debates

How do parents experience being asked to enter a child in a randomised controlled trial?

Democracy: the forgotten challenge for bioethics in the developing countries

Ethical issues relating to the banking of umbilical cord blood in Mexico

Informed recruitment in partner studies of HIV transmission: an ethical issue in couples research

developing country response to Lavery et al. "In global health research, is it legitimate to stop clinical trials early on account of their opportunity costs?

How old are you? Newborn gestational age discriminates neonatal resuscitation practices in the Italian debate

Investigational Article

Reporting of euthanasia and physician-assisted suicide in the Netherlands: descriptive study

Survey of doctors\' opinions of the legalisation of physician assisted suicide

Research understanding, attitude and awareness towards biobanking: a survey among Italian twin participants to a genetic epidemiological study

Knowledge, attitudes and practices survey on organ donation among a selected adult population of Pakistan

Technology assessment and resource allocation for predictive genetic testing: A study of the perspectives of Canadian genetic health care providers

Expression of therapeutic misconception amongst Egyptians: a qualitative pilot study

Capacity mapping of national ethics committees in the Eastern Mediterranean Region

Disagreements with implications: diverging discourses on the ethics of non-medical use of methylphenidate for performance enhancement

Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?

Post-consent assessment of dental subjects\' understanding of informed consent in oral health research in Nigeria

Impact of social stigma on the process of obtaining informed consent for genetic research on podoconiosis: a qualitative study

Assessment of the capacity to consent to treatment in patients admitted to acute medical wards

Microbicides Development Programme: Engaging the community in the standard of care debate in a vaginal microbicide trial in Mwanza, Tanzania